De Boer, Martin <br/><br/>
A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi Jews.  [electronic resource] 

 -  Journal of medical genetics  03 2018 
 - 166-172 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmedgenet-2017-105022  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Exons--genetics<br/>Female<br/>Genetic Carrier Screening<br/>Genetic Testing<br/>Granulomatous Disease, Chronic--genetics<br/>Heterozygote<br/>Humans<br/>Jews--genetics<br/>Male<br/>Mutation<br/>NADPH Oxidases--genetics<br/>Pregnancy